Consulting Wallah › Device Explorer › Other devices › Hand-held deep-tissue electromagnetic stimulator
Device Explorer · FDA GUDID · GMDN 35169

Hand-held deep-tissue electromagnetic stimulator

A battery-powered, hand-held device designed to apply an electromagnetic (EM) field to body deep tissues to help reduce pain associated with musculoskeletal/neurological disorders (e.g., arthritis, sciatica) and/or to treat soft-tissue wounds and injuries with

US‑registered devices56in commercial distribution
Companies8labelers on GUDID
Single‑use4%of device records
Sterile0%labelled sterile
Prescription54%Rx‑only share
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Share of device records

Caerus Corp.2850%
Bemer Int. Ag1425%
Bioelectronics Corporation59%
Shenzhen Nuon Medical Equipment Co., Ltd.47%
Wellness Without Limits Llc24%
Xiamen Healthpal Electronic Co., Ltd.12%
Nexstim Oyj12%
Trophy Skin, Inc12%

Top labelers

CompanyDevicesShare
Caerus Corp.2850%
Bemer Int. Ag1425%
Bioelectronics Corporation59%
Shenzhen Nuon Medical Equipment Co., Ltd.47%
Wellness Without Limits Llc24%
Xiamen Healthpal Electronic Co., Ltd.12%
Nexstim Oyj12%
Trophy Skin, Inc12%

Company = labeler of record on GUDID. 8 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NuonHealthpalNexstim NBS softwareOrthoCor MedicalTrophy SkinKT RECOVERY+ WAVEActiPatchRecoveryRxLS Pro SystemsBEMER Premium-Set EvoBEMER Basic-Set EvoBEMER Therapy SystemsBemer Therapy SystemBEMER Classic-Set Evo (B.Bed)BEMER Classic-Set Evo (B.Body)B.Box Evo

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
ILXDiathermy, Shortwave, For Use Other Than Applying Therapeuti30
NGXStimulator, Muscle, Powered, For Muscle Conditioning14
IMDPack, Hot Or Cold, Disposable13
IRTPad, Heating, Powered13
PQYNonthermal Shortwave Therapy Device Indicated For Over The C12
NFOStimulator, Transcutaneous Electrical, Aesthetic Purposes5

GMDN & GCC registration

  • GMDN code 35169 · non‑implantable
  • Single‑use 4% · sterile 0% · Rx‑only 54% · OTC 30%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

No structured size data on the register.

Use these as the dimensions to specify in a tender line.

How many hand-held deep-tissue electromagnetic stimulator products are registered in the US?

56 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Hand-held deep-tissue electromagnetic stimulator", from 8 companies. The largest labeler is Caerus Corp. with 50% of records.

Which FDA product codes apply?

ILX (Diathermy, Shortwave, For Use Other Than Applying Therapeuti), NGX (Stimulator, Muscle, Powered, For Muscle Conditioning), IMD (Pack, Hot Or Cold, Disposable), IRT (Pad, Heating, Powered)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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